CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Bortezomib-based Anthracycline-free Induction for Pediatric Relapsed ALL as a Bridge to Immunotherapy.
Bortezomib-based Anthracycline-free Induction for Pediatric Relapsed ALL as a Bridge to Immunotherapy.
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对于计划进行免疫治疗的 R/R ALL 患者,在基于 bortezomib 的治疗方案中可以安全地省略蒽环类药物。
免疫治疗可使复发/难治性急性淋巴细胞白血病(R/R ALL)患者获得持久缓解。接受免疫治疗时疾病负荷较低的患者往往长期结局更好且毒性更小。因此,需要一种诱导方案来实现较低的疾病负荷。在4药诱导方案中加入硼替佐米已被证明可使R/R ALL患者获得高缓解率。在该方案中纳入蒽环类药物可能会排除大多数患者,因为这些患者已用尽蒽环类药物的累积剂量。因此,我们的目标是评估不含蒽环类药物的硼替佐米为基础诱导方案用于R/R ALL患者。方法:我们对我中心2011年至2019年间接受硼替佐米为基础方案治疗的R/R ALL患者进行了回顾性分析。收集并分析了有关毒性和缓解率的数据。
18例R/R ALL患儿接受了以硼替佐米为基础的诱导治疗,其中13例未使用蒽环类药物。11例患者未完成诱导疗程:6例因毒性,5例因医生决定提前进行免疫治疗。发生2例治疗相关死亡事件。接受蒽环类药物治疗与未接受蒽环类药物治疗的患者在毒性方面无显著差异。10例患者达到完全缓解,其中4例患者的聚合酶链反应微小残留病低于10-4。15例患者直接进行免疫治疗:11例接受CD19CAR-T 细胞,2例接受blinatumomab,2例接受造血干细胞移植。
Immunotherapy may lead to durable remissions in patients with relapsed and refractory acute lymphoblastic leukemia (R/R ALL). Patients receiving immunotherapy with a lower disease burden tend to have improved long-term outcomes and less toxicity. Thus, an induction protocol to achieve lower disease burden is required. Bortezomib added to a 4-drug induction was shown to lead to high rates of remission in R/R ALL patients. Inclusion of anthracyclines in this protocol may preclude most patients, having maximized the cumulative dose of anthracyclines. Thus, our goal was to evaluate anthracycline-free bortezomib-based induction for patients with R/R ALL. PROCEDURE: We conducted a retrospective analysis of patients treated with bortezomib-based protocols for R/R ALL between 2011 and 2019 at our center. Data regarding toxicity and response rate was collected and analyzed.
Eighteen children with R/R ALL were treated with bortezomib-based induction, 13 of them without anthracyclines. Eleven patients did not complete the induction course: 6 due to toxicity, and 5 due to physician decision to proceed to immunotherapy early. Two events of treatment-related mortality occurred. There was no significant difference in toxicity between patients who treated with anthracycline and those who were not. Ten patients achieved complete remission, with 4 patients having polymerase-chain-reaction minimal residual disease below 10-4. Fifteen patients proceeded directly to immunotherapy: 11 patients received CD19 chimeric-antigen receptor-T-cells, 2 blinatumomab and 2 hematopoietic stem cell transplant.
Anthracyclines can be safely omitted from bortezomib-based therapies in patients with R/R ALL, when planning to proceed to immunotherapy.
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